Journal
CHEMICAL COMMUNICATIONS
Volume 56, Issue 59, Pages 8194-8197Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cc00457j
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Funding
- NFS of China [21801188]
- Shanghai Pujiang Program
- 1000 Youth Talents Plan
- Fundamental Research Funds for the Central Universities, China
- Tongji University
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A nickel-catalyzed intramolecular addition of aryl halides to 1,3-diketones was first developed. This desymmetrization reaction afforded polycyclic products bearing two tetrasubstituted centers with excellent diastereoselectivities and high yields. Moderate enantioselectivities were achieved in the presence of a chiral ligand. This transformation has great potential for the synthesis of polycyclic compounds including spiro[4,4,3,0] compounds.
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